Truncated hantavirus nucleocapsid proteins for serotyping Sin Nombre, Andes, and Laguna Negra hantavirus infections in humans and rodents

Takaaki Koma, Kumiko Yoshimatsu, Noemi Pini, David Safronetz, Midori Taruishi, Silvana Levis, Rika Endo, Kenta Shimizu, Shumpei P. Yasuda, Hideki Ebihara, Heinz Feldmann, Delia Enria, Jiro Arikawa

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

Sin Nombre virus (SNV), Andes virus (ANDV), and Laguna Negra virus (LANV) have been known as the dominant causative agents of hantavirus pulmonary syndrome (HPS). ANDV and LANV, with different patterns of pathogenicity, exist in a sympatric relationship. Moreover, there is documented evidence of person-to-person transmission of ANDV. Therefore, it is important in clinical medicine and epidemiology to know the serotype of a hantavirus causing infection. Truncated SNV, ANDV, and LANV recombinant nucleocapsid proteins (trNs) missing 99 N-terminal amino acids (trN100) were expressed using a baculovirus system, and their applicability for serotyping SNV, ANDV, and LANV infection by the use of enzyme-linked immunosorbent assays (ELISA) was examined. HPS patient sera and natural-reservoir rodent sera infected with SNV, ANDV, and LANV showed the highest optical density (OD) values for homologous trN100 antigens. Since even patient sera with lower IgM and IgG antibody titers were serotyped, the trN100s are therefore considered useful for serotyping with early-acute-phase sera. In contrast, assays testing whole recombinant nucleocapsid protein antigens of SNV, ANDV, and LANV expressed in Escherichia coli detected homologous and heterologous antibodies equally. These results indicated that a screening ELISA using an E. coli-expressed antigen followed by a serotyping ELISA using trN100s is useful for epidemiological surveillance in regions where two or more hantavirus species cocirculate.

Original languageEnglish (US)
Pages (from-to)1635-1642
Number of pages8
JournalJournal of Clinical Microbiology
Volume48
Issue number5
DOIs
StatePublished - May 1 2010
Externally publishedYes

Fingerprint

Hantavirus Infections
Hantavirus
Nucleocapsid Proteins
Serotyping
Sin Nombre virus
Rodentia
Viruses
Hantavirus Pulmonary Syndrome
Enzyme-Linked Immunosorbent Assay
Serum
Recombinant Proteins
Antigens
Escherichia coli
Heterophile Antibodies
Baculoviridae
Clinical Medicine
Virus Diseases
Immunoglobulin M
Virulence
Epidemiology

ASJC Scopus subject areas

  • Microbiology (medical)

Cite this

Truncated hantavirus nucleocapsid proteins for serotyping Sin Nombre, Andes, and Laguna Negra hantavirus infections in humans and rodents. / Koma, Takaaki; Yoshimatsu, Kumiko; Pini, Noemi; Safronetz, David; Taruishi, Midori; Levis, Silvana; Endo, Rika; Shimizu, Kenta; Yasuda, Shumpei P.; Ebihara, Hideki; Feldmann, Heinz; Enria, Delia; Arikawa, Jiro.

In: Journal of Clinical Microbiology, Vol. 48, No. 5, 01.05.2010, p. 1635-1642.

Research output: Contribution to journalArticle

Koma, T, Yoshimatsu, K, Pini, N, Safronetz, D, Taruishi, M, Levis, S, Endo, R, Shimizu, K, Yasuda, SP, Ebihara, H, Feldmann, H, Enria, D & Arikawa, J 2010, 'Truncated hantavirus nucleocapsid proteins for serotyping Sin Nombre, Andes, and Laguna Negra hantavirus infections in humans and rodents', Journal of Clinical Microbiology, vol. 48, no. 5, pp. 1635-1642. https://doi.org/10.1128/JCM.00072-10
Koma, Takaaki ; Yoshimatsu, Kumiko ; Pini, Noemi ; Safronetz, David ; Taruishi, Midori ; Levis, Silvana ; Endo, Rika ; Shimizu, Kenta ; Yasuda, Shumpei P. ; Ebihara, Hideki ; Feldmann, Heinz ; Enria, Delia ; Arikawa, Jiro. / Truncated hantavirus nucleocapsid proteins for serotyping Sin Nombre, Andes, and Laguna Negra hantavirus infections in humans and rodents. In: Journal of Clinical Microbiology. 2010 ; Vol. 48, No. 5. pp. 1635-1642.
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AU - Endo, Rika

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